Comparison of Two Extubation Techniques in Critically Ill Adult Patients (ExtubAR)
Primary Purpose
Weaning Failure, Mechanical Ventilation Complication
Status
Terminated
Phase
Not Applicable
Locations
Argentina
Study Type
Interventional
Intervention
Positive Pressure Extubation Technique
Traditional Extubation Technique
Sponsored by
About this trial
This is an interventional treatment trial for Weaning Failure focused on measuring airway extubation, extubation methods, positive pressure, positive-pressure extubation, tracheal extubation, positive-pressure ventilation, extubation complications
Eligibility Criteria
Inclusion Criteria:
- Age >18
- Invasive mechanical ventilation through an endotracheal tube,
- Successfully complete a spontaneous breathing trial
- Adequate level of consciousness (Glasgow Coma Score >8)
- Effective cough.
- Written informed consent from a relative or legal representative.
Exclusion Criteria:
- History of upper airway injury or surgery
- Previously extubated or tracheostomized
- Noninvasive ventilation (NIV) as a weaning method
- Decision to not reanimate
Sites / Locations
- Hospital Santojanni
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Positive Pressure Extubation Technique
Traditional Extubation Technique
Arm Description
ETT is removed in PSV 15/10 mode and without endotracheal suction.
ETT is removed with continuous endotracheal suction
Outcomes
Primary Outcome Measures
Number of Participants With Major Post Extubation Complications
Clinical evidence of at least one of the following:
Upper airway obstruction
Desaturation
Vomiting
Secondary Outcome Measures
Number of Participants With Minor Post Extubation Complications
Clinical evidence of at least one of the following:
Hypertension
Tachycardia
Tachypnea
Poor respiratory mechanics
Bronchospasm
Severe cough
Post obstructive pulmonary edema
Number of Participants With Overall Post Extubation Complications
Clinical evidence of at least one of the following:
Upper airway obstruction
Desaturation
Vomiting
Hypertension
Tachycardia
Tachypnea
Poor respiratory mechanics
Bronchospasm
Severe cough
Post obstructive pulmonary edema
Number of Participants With Post Extubation Pneumonia
Presence of a new radiographic infiltrate or progression of infiltrates prior to extubation and any of the following: fever, leukocytosis (greater than 10,000 / mm3) or leukopenia (less than 4,000 / mm3) compared to the value prior to extubation and increase in the amount or change in the quality of tracheobronchial secretions.
Number of Participants With Extubation Failure
Use of Non Invasive Ventilation to treat the failure or need of reintubation.
Number of Participants That Required Reintubation
Need of reintubation.
Full Information
NCT ID
NCT03918811
First Posted
April 14, 2019
Last Updated
January 20, 2021
Sponsor
Hospital Donación Francisco Santojanni
Collaborators
Matías Bertozzi, Marco Bezzi, Silvina Borello, Daniela Castro, Victoria Di Giorgio, Mariana Aguirre, Karina Miralles, Diego Noval, Sebastián Fredes, Eliana Wilhelm, Mauricio Zakimchuk, Julián Buffarini Cignoli, Mariana Bernardini, Leticia Rey, Valeria Pieroni, Pablo D´Annunzio, Gustavo Plotnikow, Romina Prato, Matías Lompizano, María Guaymas, Matías Accoce, Javier Dorado, Gimena Cardoso, Patricia Torres, Vanesa Pavlotsky, Emiliano Navarro, Eliana Markman, Paula Di Nardo, Ivonne Kunzi Steyer, Carolina Thomsen, Cecilia Palacios, Mariela Davies, Mercedes Ruffo, Victoria Leon, Fernando Tapia
1. Study Identification
Unique Protocol Identification Number
NCT03918811
Brief Title
Comparison of Two Extubation Techniques in Critically Ill Adult Patients
Acronym
ExtubAR
Official Title
Comparison of Two Extubation Techniques in Critically Ill Adult Patients (ExtubAR Trial): Randomized Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Terminated
Why Stopped
Due to the outbreak of the SARS-CoV-2 pandemic in Argentina and the lack of information about the potential risks of contamination from extubation and aerosolization, we stopped recruiting patients before achieving the predefined sample size.
Study Start Date
April 1, 2019 (Actual)
Primary Completion Date
March 26, 2020 (Actual)
Study Completion Date
March 26, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Donación Francisco Santojanni
Collaborators
Matías Bertozzi, Marco Bezzi, Silvina Borello, Daniela Castro, Victoria Di Giorgio, Mariana Aguirre, Karina Miralles, Diego Noval, Sebastián Fredes, Eliana Wilhelm, Mauricio Zakimchuk, Julián Buffarini Cignoli, Mariana Bernardini, Leticia Rey, Valeria Pieroni, Pablo D´Annunzio, Gustavo Plotnikow, Romina Prato, Matías Lompizano, María Guaymas, Matías Accoce, Javier Dorado, Gimena Cardoso, Patricia Torres, Vanesa Pavlotsky, Emiliano Navarro, Eliana Markman, Paula Di Nardo, Ivonne Kunzi Steyer, Carolina Thomsen, Cecilia Palacios, Mariela Davies, Mercedes Ruffo, Victoria Leon, Fernando Tapia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Orotracheal extubation consists in the removal of the endotracheal tube (ETT) when it is no longer required. This procedure may carry a considerable risk of complications and extubation failure. The literature points out two methods of extubation: the traditional method and the positive pressure method.
In a noninferiority clinical trial it was demonstrated that EOT with positive pressure and without endotracheal suction was a safe technique and could be better than traditional extubation. Although prior studies reported better clinical outcomes with the positive pressure extubation technique, its superiority has not been deeply studied yet. Therefore, the objective of our study is to determine whether the positive pressure OTE technique, compared with the traditional OTE technique, reduces the incidence of major postextubation complications (up to 60 minutes) in critically ill adult patients.
Detailed Description
Design: Multicenter randomized controlled clinical trial Methods: Critically ill adult subjects on invasive mechanical ventilation who met extubation criteria will be included. Will be randomly assigned to positive-pressure extubation (n=389) or to traditional extubation (n=389).
The main variable will be incidence of major complications.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Weaning Failure, Mechanical Ventilation Complication
Keywords
airway extubation, extubation methods, positive pressure, positive-pressure extubation, tracheal extubation, positive-pressure ventilation, extubation complications
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
superiority
Masking
InvestigatorOutcomes Assessor
Masking Description
Due to the nature of the intervention, blinding of the subject and the operators responsible for extubation is not possible. The person in charge of data statistical analysis and the evaluator who assess and record outcome measures will be blinded to the allocated intervention.
Allocation
Randomized
Enrollment
725 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Positive Pressure Extubation Technique
Arm Type
Experimental
Arm Description
ETT is removed in PSV 15/10 mode and without endotracheal suction.
Arm Title
Traditional Extubation Technique
Arm Type
Active Comparator
Arm Description
ETT is removed with continuous endotracheal suction
Intervention Type
Procedure
Intervention Name(s)
Positive Pressure Extubation Technique
Intervention Description
Positive-pressure extubation is performed by only one operator. Ventilator parameters are set to pressure support ventilation mode, with an inspiratory pressure of 15 cm H2O and PEEP of 10 cm H2O. Then, the cuff is deflated, and the ETT is removed without endotracheal suction. Once the ETT is removed, a suction catheter is introduced through the mouth to suction secretions drawn to the oropharynx by the air flow from the ventilator passing between the ETT and the larynx.
Intervention Type
Procedure
Intervention Name(s)
Traditional Extubation Technique
Intervention Description
Traditional extubation is performed by 2 operators. Without reconnection to the ventilator, the closed suction system catheter is introduced by one of the operators into the ETT and suctioning is initiated. The cuff is immediately deflated by the other operator, and the ETT is removed with continuous endotracheal suction during the whole procedure by the first operator.
Primary Outcome Measure Information:
Title
Number of Participants With Major Post Extubation Complications
Description
Clinical evidence of at least one of the following:
Upper airway obstruction
Desaturation
Vomiting
Time Frame
Within15 minutes after extubation.
Secondary Outcome Measure Information:
Title
Number of Participants With Minor Post Extubation Complications
Description
Clinical evidence of at least one of the following:
Hypertension
Tachycardia
Tachypnea
Poor respiratory mechanics
Bronchospasm
Severe cough
Post obstructive pulmonary edema
Time Frame
Hypertension, Tachycardia, Tachypnea or Poor Respiratory Mechanics, within 15 minutes after extubation. Bronchospasm, Severe cough or Post Obstructive Pulmonary Edema, within 60 minutes after extubation.
Title
Number of Participants With Overall Post Extubation Complications
Description
Clinical evidence of at least one of the following:
Upper airway obstruction
Desaturation
Vomiting
Hypertension
Tachycardia
Tachypnea
Poor respiratory mechanics
Bronchospasm
Severe cough
Post obstructive pulmonary edema
Time Frame
Upper airway obstruction, Desaturation, Vomiting, Hypertension, Tachycardia, Tachypnea, Poor Respiratory Mechanics, within 15 minutes after extubation. Bronchospasm, Severe cough or Post Obstructive Pulmonary Edema, within 60 minutes after extubation.
Title
Number of Participants With Post Extubation Pneumonia
Description
Presence of a new radiographic infiltrate or progression of infiltrates prior to extubation and any of the following: fever, leukocytosis (greater than 10,000 / mm3) or leukopenia (less than 4,000 / mm3) compared to the value prior to extubation and increase in the amount or change in the quality of tracheobronchial secretions.
Time Frame
Within 72 hours after extubation.
Title
Number of Participants With Extubation Failure
Description
Use of Non Invasive Ventilation to treat the failure or need of reintubation.
Time Frame
Within 72 hours after extubation.
Title
Number of Participants That Required Reintubation
Description
Need of reintubation.
Time Frame
Within 72 hours after extubation.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age >18
Invasive mechanical ventilation through an endotracheal tube,
Successfully complete a spontaneous breathing trial
Adequate level of consciousness (Glasgow Coma Score >8)
Effective cough.
Written informed consent from a relative or legal representative.
Exclusion Criteria:
History of upper airway injury or surgery
Previously extubated or tracheostomized
Noninvasive ventilation (NIV) as a weaning method
Decision to not reanimate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mauro F Andreu, Prof
Organizational Affiliation
Hospital Santojanni
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Santojanni
City
Buenos Aires
ZIP/Postal Code
1408
Country
Argentina
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
25425709
Citation
Andreu MF, Salvati IG, Donnianni MC, Ibanez B, Cotignola M, Bezzi M. Effect of applying positive pressure with or without endotracheal suctioning during extubation: a laboratory study. Respir Care. 2014 Dec;59(12):1905-11. doi: 10.4187/respcare.03121. Epub 2014 Nov 25.
Results Reference
background
PubMed Identifier
30914493
Citation
Andreu MF, Dotta ME, Bezzi MG, Borello S, Cardoso GP, Dib PC, Garcia Schustereder SL, Galloli AM, Castro DR, Di Giorgio VL, Villalba FJ, Bertozzi MN, Carballo JM, Martin MC, Brovia CC, Pita MC, Pedace MP, De Benedetto MF, Delli Carpini J, Aguirre P, Montero G. Safety of Positive Pressure Extubation Technique. Respir Care. 2019 Aug;64(8):899-907. doi: 10.4187/respcare.06541. Epub 2019 Mar 26.
Results Reference
background
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Comparison of Two Extubation Techniques in Critically Ill Adult Patients
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